Beta-amyloid deposition around hepatic bile ducts is a novel pathobiological and diagnostic feature of biliary atresia

Biliary atresia (BA) is a poorly understood and devastating obstructive bile duct disease of newborns. It is often diagnosed late, is incurable and frequently requires liver transplantation. In this study, we aimed to investigate the underlying pathogenesis and molecular signatures associated with B...

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Veröffentlicht in:Journal of hepatology 2020-12, Vol.73 (6), p.1391-1403
Hauptverfasser: Babu, Rosana Ottakandathil, Lui, Vincent Chi Hang, Chen, Yan, Yiu, Rachel Sze Wan, Ye, Yongqin, Niu, Ben, Wu, Zhongluan, Zhang, Ruizhong, Yu, Michelle On Na, Chung, Patrick Ho Yu, Wong, Kenneth Kak Yuen, Xia, Huimin, Zhang, Michael Qi, Wang, Bin, Lendahl, Urban, Tam, Paul Kwong Hang
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Sprache:eng
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Zusammenfassung:Biliary atresia (BA) is a poorly understood and devastating obstructive bile duct disease of newborns. It is often diagnosed late, is incurable and frequently requires liver transplantation. In this study, we aimed to investigate the underlying pathogenesis and molecular signatures associated with BA. We combined organoid and transcriptomic analysis to gain new insights into BA pathobiology using patient samples and a mouse model of BA. Liver organoids derived from patients with BA and a rhesus rotavirus A-infected mouse model of BA, exhibited aberrant morphology and disturbed apical-basal organization. Transcriptomic analysis of BA organoids revealed a shift from cholangiocyte to hepatocyte transcriptional signatures and altered beta-amyloid-related gene expression. Beta-amyloid accumulation was observed around the bile ducts in BA livers and exposure to beta-amyloid induced the aberrant morphology in control organoids. The novel observation that beta-amyloid accumulates around bile ducts in the livers of patients with BA has important pathobiological implications, as well as diagnostic potential. Biliary atresia is a poorly understood and devastating obstructive bile duct disease of newborns. It is often diagnosed late, is incurable and frequently requires liver transplantation. Using human and mouse ‘liver mini-organs in the dish’, we unexpectedly identified beta-amyloid deposition – the main pathological feature of Alzheimer's disease and cerebral amyloid angiopathy – around bile ducts in livers from patients with biliary atresia. This finding reveals a novel pathogenic mechanism that could have important diagnostic and therapeutic implications. [Display omitted] •Liver organoids from patients with BA exhibited aberrant morphology and disturbed apical-basal organization.•Transcriptomic analysis of BA organoids revealed a shift from cholangiocyte to hepatocyte transcriptional signatures.•Beta-amyloid accumulation was observed around the bile ducts in BA livers.•Exposure to beta-amyloid induced aberrant morphology in control organoids.•Beta-amyloid accumulation represents a novel finding with pathobiological implications and diagnostic potential for BA.
ISSN:0168-8278
1600-0641
1600-0641
DOI:10.1016/j.jhep.2020.06.012